ouabain and Spherocytosis, Hereditary

ouabain has been researched along with Spherocytosis, Hereditary in 17 studies

Research

Studies (17)

Timeframe	Studies, this research(%)	All Research%
pre-1990	17 (100.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	0 (0.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
JACOB, HS; JANDL, JH	1
MOHLER, DN	1
Jacob, HS; Karnovsky, ML	1
Kramer, S; Krawtiz, P; Metz, J; Viljoen, E; Zail, SS	1
Yawata, Y; Yoshimoto, M	1
Gjønnes, G; Godal, HC; Ruyter, R	1
Johnsson, R; Salminen, S	1
Bruckdorfer, R; Chailley, B; Dagher, G; Delaunay, J; Feo, C; Fischer, S; Garay, R; Piau, JP	1
Harnchonboth, K; Mandel, EE; Minn, SK	1
Gatlin, P; Hansotia, P; Mazza, JJ	1
Kurashina, S; Nakao, K; Nakao, M	1
Wiley, JS	2
Esselborn, H; Löhr, GW	1
Parker, JC; Welt, LG	1
Mayman, D; Zipursky, A	1
Reed, CF; Swisher, SN	1

Reviews

2 review(s) available for ouabain and Spherocytosis, Hereditary

Article	Year
[Hereditary spherocytosis]. Blut, 1970, Volume: 20, Issue:3 Topics: Adenosine Triphosphatases; Anemia; Cell Membrane Permeability; Erythrocyte Aging; Erythrocytes; Erythropoiesis; Glycolysis; Humans; Hyperbilirubinemia; Jaundice; Osmotic Fragility; Ouabain; Phospholipids; Reticulocytes; Sodium; Spherocytosis, Hereditary; Splenectomy; Splenomegaly	1970
Pathological alterations of cation movements in red blood cells. Archives of internal medicine, 1972, Volume: 129, Issue:2 Topics: Adenosine Triphosphatases; Adenosine Triphosphate; Anemia, Hemolytic; Anemia, Sickle Cell; Biological Transport, Active; Cell Membrane Permeability; Elliptocytosis, Hereditary; Erythrocyte Aging; Erythrocytes; Erythrocytes, Abnormal; Heinz Bodies; Hemoglobinopathies; Hemolysis; Humans; Hydrolysis; Lipid Metabolism, Inborn Errors; Lipids; Malaria; Membrane Potentials; Ouabain; Potassium; Sodium; Spherocytosis, Hereditary; Sulfhydryl Compounds; Sulfhydryl Reagents	1972

Article

Year

[Hereditary spherocytosis].

Blut, 1970, Volume: 20, Issue:3

Topics: Adenosine Triphosphatases; Anemia; Cell Membrane Permeability; Erythrocyte Aging; Erythrocytes; Erythropoiesis; Glycolysis; Humans; Hyperbilirubinemia; Jaundice; Osmotic Fragility; Ouabain; Phospholipids; Reticulocytes; Sodium; Spherocytosis, Hereditary; Splenectomy; Splenomegaly

1970

Pathological alterations of cation movements in red blood cells.

Archives of internal medicine, 1972, Volume: 129, Issue:2

Topics: Adenosine Triphosphatases; Adenosine Triphosphate; Anemia, Hemolytic; Anemia, Sickle Cell; Biological Transport, Active; Cell Membrane Permeability; Elliptocytosis, Hereditary; Erythrocyte Aging; Erythrocytes; Erythrocytes, Abnormal; Heinz Bodies; Hemoglobinopathies; Hemolysis; Humans; Hydrolysis; Lipid Metabolism, Inborn Errors; Lipids; Malaria; Membrane Potentials; Ouabain; Potassium; Sodium; Spherocytosis, Hereditary; Sulfhydryl Compounds; Sulfhydryl Reagents

1972

Other Studies

15 other study(ies) available for ouabain and Spherocytosis, Hereditary

Article	Year
INCREASED CELL MEMBRANE PERMEABILITY IN THE PATHOGENESIS OF HEREDITARY SPHEROCYTOSIS. The Journal of clinical investigation, 1964, Volume: 43 Topics: Ankyrins; Biological Transport; Cardiac Glycosides; Cell Membrane Permeability; Erythrocytes; Glucose; Glycolysis; Hemolysis; Humans; Lactates; Metabolism; Osmosis; Ouabain; Phosphates; Potassium; Sodium; Spherocytosis, Hereditary; Splenectomy; Sucrose	1964
ADENOSINE TRIPHOSPHATE METABOLISM IN HEREDITARY SPHEROCYTOSIS. The Journal of clinical investigation, 1965, Volume: 44 Topics: Adenosine Triphosphate; Ankyrins; Biological Transport; Glucose; Hemolysis; Hydrogen-Ion Concentration; Metabolism; Ouabain; Pharmacology; Spherocytosis, Hereditary	1965
Concomitant alterations of sodium flux and membrane phospholipid metabolism in red blood cells: studies in hereditary spherocytosis. The Journal of clinical investigation, 1967, Volume: 46, Issue:2 Topics: Biological Transport; Cell Membrane; Chromatography, Thin Layer; Erythrocytes; Humans; Ions; Osmosis; Ouabain; Phosphatidylethanolamines; Phospholipids; Radioisotopes; Sodium; Spherocytosis, Hereditary	1967
Atypical hereditary spherocytosis: biochemical studies and sites of erythrocyte destruction. British journal of haematology, 1967, Volume: 13, Issue:3 Topics: Adenosine Triphosphate; Adolescent; Adult; Aged; Bilirubin; Biochemical Phenomena; Biochemistry; Blood Cell Count; Culture Techniques; Female; Glucose; Hemoglobinometry; Hemolysis; Humans; Immune Sera; Male; Osmotic Fragility; Ouabain; Reticulocytes; Spherocytosis, Hereditary; Spleen	1967
[Increased ouabain-insensitive sodium efflux in leaky red cell membranes of the patients with hereditary spherocytosis]. Nihon Ketsueki Gakkai zasshi : journal of Japan Haematological Society, 1982, Volume: 45, Issue:3 Topics: Adenosine Triphosphatases; Ca(2+) Mg(2+)-ATPase; Cell Membrane Permeability; Erythrocyte Membrane; Erythrocytes; Humans; Ouabain; Sodium; Sodium-Potassium-Exchanging ATPase; Spherocytosis, Hereditary	1982
Failure of ouabain to influence the osmotic fragility in hereditary spherocytosis. Scandinavian journal of haematology, 1982, Volume: 28, Issue:3 Topics: Carrier State; Hemolysis; Humans; Osmotic Fragility; Ouabain; Spherocytosis, Hereditary	1982
Effect of ouabain on osmotic resistance and monovalent cation transport of red cells in hereditary spherocytosis. Scandinavian journal of haematology, 1980, Volume: 25, Issue:4 Topics: Adolescent; Adult; Biological Transport; Cations, Monovalent; Child; Child, Preschool; Erythrocytes; Humans; Osmotic Fragility; Ouabain; Spherocytosis, Hereditary	1980
Evidence for imbalanced furosemide-sensitive Na+, K+ cotransport in hereditary stomatocytosis. Scandinavian journal of haematology, 1981, Volume: 27, Issue:5 Topics: Cations; Cell Membrane Permeability; Erythrocyte Membrane; Erythrocytes; Female; Furosemide; Humans; Male; Membrane Lipids; Membrane Proteins; Osmolar Concentration; Ouabain; Potassium; Sodium; Spherocytosis, Hereditary	1981
Combined effect of dextrose and sodium chloride on red cell osmotic fragility. American journal of hematology, 1978, Volume: 5, Issue:1 Topics: Blood Glucose; Erythrocyte Membrane; Erythrocytes; Glucose; Hemolysis; Humans; Lithium; Osmotic Fragility; Ouabain; Potassium Chloride; Sodium Chloride; Spherocytosis, Hereditary; Sucrose	1978
Diphenylhydantoin and fragility of erythrocytes in normal subjects and in patients with hereditary spherocytic anemia. American journal of clinical pathology, 1975, Volume: 64, Issue:1 Topics: Adolescent; Adult; Cell Membrane Permeability; Child; Erythrocytes; Hemolysis; Humans; Hypotonic Solutions; Osmotic Fragility; Ouabain; Phenytoin; Sodium Chloride; Spherocytosis, Hereditary	1975
Adenosinetriphosphatase activity of erythrocyte membrane in hereditary spherocytosis. Life sciences, 1967, Mar-15, Volume: 6, Issue:6 Topics: Adenosine Triphosphatases; Cell Membrane; Erythrocytes; Humans; In Vitro Techniques; Ouabain; Potassium; Sodium; Spherocytosis, Hereditary	1967
Inheritance of an increased sodium pump in human red cells. Nature, 1969, Mar-29, Volume: 221, Issue:5187 Topics: Adenosine Triphosphatases; Biological Transport, Active; Depression, Chemical; Erythrocytes; Humans; Kinetics; Molecular Biology; Mutation; Ouabain; Sodium; Spherocytosis, Hereditary	1969
Co-ordinated increase of sodium leak and sodium pump in hereditary spherocytosis. British journal of haematology, 1972, Volume: 22, Issue:5 Topics: Adenosine Triphosphatases; Biological Transport, Active; Erythrocytes; Erythrocytes, Abnormal; Humans; Ouabain; Sodium; Sodium Isotopes; Spherocytosis, Hereditary; Splenectomy	1972
Hereditary spherocytosis: the metabolism of erythrocytes in the peripheral blood and in the splenic pulp. British journal of haematology, 1974, Volume: 27, Issue:2 Topics: Adenosine Triphosphatases; Biological Transport, Active; Cell Membrane Permeability; Chromium Radioisotopes; Erythrocytes; Humans; Osmotic Fragility; Ouabain; Phosphorus Radioisotopes; Potassium; Reticulocytes; Sodium; Sodium Isotopes; Spherocytosis, Hereditary; Spleen; Splenectomy	1974
Erythrocyte lipid loss in hereditary spherocytosis. The Journal of clinical investigation, 1966, Volume: 45, Issue:5 Topics: Erythrocytes; Glucose; Humans; In Vitro Techniques; Lipids; Ouabain; Spherocytosis, Hereditary; Splenectomy	1966